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nsv6565934

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,039

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 85 SVs from 22 studies. See in: genome view    
    Submitted genomic113,264,593-113,265,631Question Mark
    Overlapping variant regions from other studies: 85 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):116,026,873-116,027,911Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6565934Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9113,264,593113,265,631
    nsv6565934RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9116,026,873116,027,911

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18279639inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18279639Submitted genomicNC_000009.12:g.113
    264593_113265631in
    v
    GRCh38 (hg38)NC_000009.12Chr9113,264,593113,265,631
    nssv18279639RemappedPerfectNC_000009.11:g.116
    026873_116027911in
    v
    GRCh37.p13First PassNC_000009.11Chr9116,026,873116,027,911

    No validation data were submitted for this variant

    No clinical assertion data were submitted for this variant

    Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

    Genotype Information

    Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
    nssv18279639<0.001334964
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